Simone Sampaolo

1.8k total citations
75 papers, 1.2k citations indexed

About

Simone Sampaolo is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Simone Sampaolo has authored 75 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 22 papers in Neurology and 18 papers in Physiology. Recurrent topics in Simone Sampaolo's work include Lysosomal Storage Disorders Research (10 papers), Mitochondrial Function and Pathology (8 papers) and Cardiomyopathy and Myosin Studies (7 papers). Simone Sampaolo is often cited by papers focused on Lysosomal Storage Disorders Research (10 papers), Mitochondrial Function and Pathology (8 papers) and Cardiomyopathy and Myosin Studies (7 papers). Simone Sampaolo collaborates with scholars based in Italy, United States and Germany. Simone Sampaolo's co-authors include Giuseppe Di Iorio, Mariarosa Anna Beatrice Melone, Filomena Napolitano, Francesco Tomasello, Jorge Cervós‐Navarro, Teresa Esposito, Vincenzo Albanese, Fernando Gianfrancesco, Ángel Campos‐Barros and S. Migliaresi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

Simone Sampaolo

74 papers receiving 1.1k citations

Peers

Simone Sampaolo
Young Seok Park South Korea
Simone Sampaolo
Citations per year, relative to Simone Sampaolo Simone Sampaolo (= 1×) peers Young Seok Park

Countries citing papers authored by Simone Sampaolo

Since Specialization
Citations

This map shows the geographic impact of Simone Sampaolo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Simone Sampaolo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Sampaolo more than expected).

Fields of papers citing papers by Simone Sampaolo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Simone Sampaolo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Simone Sampaolo. The network helps show where Simone Sampaolo may publish in the future.

Co-authorship network of co-authors of Simone Sampaolo

This figure shows the co-authorship network connecting the top 25 collaborators of Simone Sampaolo. A scholar is included among the top collaborators of Simone Sampaolo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Simone Sampaolo. Simone Sampaolo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Napolitano, Filomena, Gianmarco Abbadessa, Maria Ravo, et al.. (2025). Serum miRNAs as biomarkers in Neurofibromatosis 1: New promising findings. Journal of the Neurological Sciences. 476. 123643–123643. 1 indexed citations
2.
Monda, Emanuele, Michele Lioncino, Martina Caiazza, et al.. (2023). Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes. International Journal of Molecular Sciences. 24(10). 9108–9108. 3 indexed citations
3.
Lioncino, Michele, Emanuele Monda, Martina Caiazza, et al.. (2023). Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies. Circulation Genomic and Precision Medicine. 16(4). 412–414. 1 indexed citations
4.
Polverino, Francesca, et al.. (2023). Diagnosis of amyotrophic lateral sclerosis by respiratory function test. Multidisciplinary Respiratory Medicine. 18(1). 941–941. 1 indexed citations
5.
Napolitano, Filomena, Chiara Terracciano, Maria Teresa Gentile, et al.. (2022). Genotype-Phenotype Correlations in Neurofibromatosis Type 1: Identification of Novel and Recurrent NF1 Gene Variants and Correlations with Neurocognitive Phenotype. Genes. 13(7). 1130–1130. 15 indexed citations
6.
Petracca, Martina, Anna Rita Bentivoglio, Serenella Servidei, et al.. (2021). Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement. Genes. 12(3). 344–344. 7 indexed citations
7.
Puoti, Gianfranco, et al.. (2020). A novel missense mutation in CAV3 gene in an Italian family with persistent hyperCKemia, myalgia and hypercholesterolemia: Double-trouble. Clinical Neurology and Neurosurgery. 191. 105687–105687. 7 indexed citations
8.
Liguori, Sara, et al.. (2018). Musculoskeletal impairment and functional limitations in a patient affected by mutation in the laminin a-5 gene.. PubMed. 33(2). 117–118. 1 indexed citations
9.
Terracciano, Chiara, Filomena Napolitano, Alessandra D’Amico, et al.. (2018). Late adult-onset adrenomyeloneuropathy evolving with atypical severe frontal lobe syndrome: Importance of neuroimaging. Radiology Case Reports. 14(3). 309–314. 2 indexed citations
10.
Pascarella, Angelo, Chiara Terracciano, Luca Lombardi, et al.. (2017). Vacuolated PAS‐positive lymphocytes as an hallmark of Pompe disease and other myopathies related to impaired autophagy. Journal of Cellular Physiology. 233(8). 5829–5837. 13 indexed citations
11.
Migliaresi, S., Giuseppe Di Iorio, A. Ammendola, et al.. (2011). Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia. Reumatismo. 53(1). 26–32. 6 indexed citations
12.
Formicola, Daniela, Simone Sampaolo, Daria Diodato, et al.. (2010). Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility. BMC Medical Genetics. 11(1). 103–103. 39 indexed citations
13.
Sampaolo, Simone, Antonio Varone, Daria Diodato, et al.. (2007). C.P.1.01 Congenital fiber type disproportion and noncompaction cardiomyopathy in a patient. Neuromuscular Disorders. 17(9-10). 834–834. 1 indexed citations
14.
Melone, Mariarosa Anna Beatrice, Alessandra Tessa, Stefania Petrini, et al.. (2004). Revelation of a New Mitochondrial DNA Mutation (G12147A) in a MELAS/MERFF Phenotype. Archives of Neurology. 61(2). 269–269. 44 indexed citations
15.
Puoti, Gianfranco, Simone Sampaolo, F. Carrara, et al.. (2003). Brain cysts associated with mutation in the Aristaless related homeobox gene, ARX. Journal of Medical Genetics. 40(11). 863–863. 2 indexed citations
16.
Melone, Mariarosa Anna Beatrice, Giuseppe Di Fede, Gianfranco Peluso, et al.. (2002). Abnormal Accumulation of tTGase Products in Muscle and Erythrocytes of Chorea-Acanthocytosis Patients. Journal of Neuropathology & Experimental Neurology. 61(10). 841–848. 13 indexed citations
17.
Mazzei, R., F. L. Conforti, A. Magariello, et al.. (2002). A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis. Journal of Neurology. 249(10). 1398–1400. 14 indexed citations
18.
Iorio, Giuseppe Di, et al.. (1993). Familial amyloidotic polyneuropathy: Description of an Italian kindred. The Italian Journal of Neurological Sciences. 14(4). 303–309. 3 indexed citations
19.
Heye, N., et al.. (1993). Morphometrical Evaluation of Triflusal in Brain Infarction. PubMed. 57. 53–55. 4 indexed citations
20.
Albanese, Valentina Erminia, Francesco Tomasello, Simone Sampaolo, & Piero Picozzi. (1982). Neuroradiological findings in multiloculated hydrocephalus. Acta Neurochirurgica. 60(3-4). 297–311. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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